Evidence map›Paper›PMID 21785676›Full record

ArticleNeurology international2011

Amyotrophic lateral sclerosis: one or multiple causes?

Aline Furtado Bastos, Marco Orsini, Dionis Machado, Mariana Pimentel Mello, Sergio Nader, Júlio Guilherme Silva, Antonio M da Silva Catharino, Marcos R G de Freitas, Alessandra Pereira, Luciane Lacerda Pessoa and 4 more

Abstract read
In one paragraph

Article in Neurology international, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Neuromuscular Junction Dismantling in Amyotrophic Lateral Sclerosis.International journal of molecular sciences · 2017
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Amyotrophic lateral sclerosis: a dying motor unit?Frontiers in aging neuroscience · 2013
    Article
  14. Article
  15. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Aline Furtado BastosSerra dos Órgãos University, Teresópolis, Rio de Janeiro;
Marco Orsini
Dionis Machado
Mariana Pimentel Mello
Sergio Nader
Júlio Guilherme Silva
Antonio M da Silva Catharino
Marcos R G de Freitas
Alessandra Pereira
Luciane Lacerda Pessoa
Flavio R Sztajnbok
Marco Araújo Leite
Osvaldo J M Nascimento
Victor Hugo Bastos

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Amyotrophic lateral sclerosis (ALS) is the most common form of motor neuron disease in the adulthood, and it is characterized by rapid and progressive compromise of the upper and lower motor neurons. The majority of the cases of ALS are classified as sporadic and, until now, a specific cause for these cases still is unknown. To present the different hypotheses on the etiology of ALS. It was carried out a search in the databases: Bireme, Scielo and Pubmed, in the period of 1987 to 2011, using the following keywords: Amyotrophic lateral sclerosis, motor neuron disease, etiology, causes and epidemiology and its similar in Portuguese and Spanish. It did not have consensus as regards the etiology of ALS. Researches demonstrates evidences as regards intoxication by heavy metals, environmental and occupational causes, genetic mutations (superoxide dismutase 1), certain viral infections and the accomplishment of vigorous physical activity for the development of the disease. There is still no consensus regarding the involved factors in the etiology of ALS. In this way, new research about these etiologies are necessary, for a better approach of the patients, promoting preventive programs for the disease and improving the quality of life of the patients.

Indexed as

amyotrophic lateral sclerosisetiologyhypothesismotor neuron diseaseneuromuscular Diseasesreview.

Identifiers

PMID21785676
PMCPMC3141115

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.